A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512590



Internal ID15852015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52385327..52388153hg38UCSC Ensembl
Outerchr19:52888580..52891406hg19UCSC Ensembl
Outerchr19:57580392..57583218hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382827
hg192827
hg182827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625201
Samples1
Known GenesZNF880
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512590
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer